0000000000362296

AUTHOR

Cheng-wei Ju

0000-0002-2250-8548

showing 13 related works from this author

Negatively Curved Nanographene with Heptagonal and [5]Helicene Units

2020

Negatively curved nanographene (NG) 4, having two heptagons and a [5]helicene, was unexpectedly obtained by aryl rearrangement and stepwise cyclodehydrogenations. X-ray crystallography confirmed the saddle-shaped structures of intermediate 3 and NG 4. The favorability of rearrangement over helicene formation following radical cation or arenium cation mechanisms is supported by theoretical calculations. NG 4 demonstrates a reversible mechanochromic color change and solid-state emission, presumably benefiting from its loose crystal packing. After resolution by chiral high-performance liquid chromatography, the circular dichroism spectra of enantiomers 4-(P) and 4-(M) were measured and showed …

[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]CommunicationArylResolution (electron density)General Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCrystalchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryRadical ionHelicene[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Arenium ionHeptagonEnantiomer[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]ComputingMilieux_MISCELLANEOUS
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Amplification of Dissymmetry Factors in π-Extended [7]- and [9]Helicenes

2021

International audience; $\pi$-Extended helicenes constitute an important class of polycyclic aromatic hydrocarbons with intrinsic chirality. Herein, we report the syntheses of $\pi$extended [7]helicene $4$ and $\pi$-extended [9]helicene $6$ through regioselective cyclodehydrogenation in high yields, where a "prefusion" strategy plays a key role in preventing undesirable aryl rearrangements. The unique helical structures are unambiguously confirmed by X-ray crystal structure analysis. Compared to the parent pristine [7]helicene and [9]helicene, these novel $\pi$-extended helicenes display significantly improved photophysical properties, with a quantum yield of 0.41 for $6$. After optical res…

Models MolecularMolecular StructureChemistryArylRegioselectivityQuantum yieldStereoisomerismGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciences3. Good healthchemistry.chemical_compoundCrystallographyColloid and Surface ChemistryHelicene[CHIM]Chemical SciencesPolycyclic CompoundsEnantiomerLuminescenceChirality (chemistry)
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From Hexaphenylbenzene to 1,2,3,4,5,6-Hexacyclohexylcyclohexane

2020

The hydrogenation of hexaphenylbenzene was studied, affording novel partially hydrogenated hexacyclohexylbenzene (HCB) as well as fully hydrogenated 1,2,3,4,5,6-hexacyclohexylcyclohexane (HCC) as an unprecedented “oligocyclohexyl” molecule. The reaction process was analyzed by mass spectrometry with atmospheric pressure chemical ionization and high-performance liquid chromatography. From a crude product mixture, two different crystals with flake- and block-shapes could be grown and analyzed by X-ray crystallography, revealing their structures as HCB and HCC. While a geared arrangement of cyclohexyl substitutes was found in HCB, two isomeric structures were identified in HCC crystal with cha…

CyclohexaneCommunicationAtmospheric-pressure chemical ionizationGeneral ChemistryMass spectrometryBiochemistryCatalysisCrystalchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryX-ray crystallographyMoleculeHexaphenylbenzeneJournal of the American Chemical Society
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A Highly Luminescent Nitrogen-Doped Nanographene as an Acid- and Metal-Sensitive Fluorophore for Optical Imaging.

2021

Dibenzo[hi,st]ovalene (DBOV) has excellent photophysical properties, including strong fluorescence and high ambient stability. Moreover, the optical blinking properties of DBOV have enabled optical super-resolution single-molecule localization microscopy with an imaging resolution beyond the diffraction limit. Various organic and inorganic fluorescent probes have been developed for super-resolution imaging, but those sensitive to pH and/or metal ions have remained elusive. Here, we report a diaza-derivative of DBOV (N-DBOV), synthesized in eight steps with a total yield of 15%. Nitrogen (N)-bearing zigzag edges were formed through oxidative cyclization of amino groups in the last step. UV-v…

IONSFluorophoreNitrogenMetal ions in aqueous solutionIronOvalenePhotochemistryOXIDATIONBiochemistryCatalysisFluorescence spectroscopyArticlechemistry.chemical_compoundColloid and Surface ChemistryMicroscopyFLUORESCENCEFluorescent DyesCONSTRUCTIONMolecular StructureChemistryDERIVATIVESWARPED NANOGRAPHENEGeneral ChemistryFluorescenceNanostructuresLuminescent MeasurementsCHEMOSENSORGraphiteN-HETEROCYCLESCyclic voltammetryAQUEOUS-MEDIUMLuminescenceSYSTEMCopperJournal of the American Chemical Society
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CCDC 2047542: Experimental Crystal Structure Determination

2021

Related Article: Zijie Qiu, Cheng-Wei Ju, Lucas Frédéric, Yunbin Hu, Dieter Schollmeyer, Grégory Pieters, Klaus Müllen, Akimitsu Narita|2021|J.Am.Chem.Soc.|143|4661|doi:10.1021/jacs.0c13197

2124-di-t-butyldibenzo[fgij]phenanthro[3'4':910]pyreno[54321-pqrst]naphtho[12-a]pentapheneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2004421: Experimental Crystal Structure Determination

2020

Related Article: Zijie Qiu, Sobi Asako, Yunbin Hu, Cheng-Wei Ju, Thomas Liu, Loïc Rondin, Dieter Schollmeyer, Jean-Sébastien Lauret, Klaus Müllen, Akimitsu Narita|2020|J.Am.Chem.Soc.|142|14814|doi:10.1021/jacs.0c05504

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters1823-di-t-butyl-1213-ethenocyclohepta[uvwxyz]dibenzo[45:67]cyclohepta[123-gh]phenanthro[9101-jkl]hexahelicene dichloromethane solvateExperimental 3D Coordinates
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CCDC 2021692: Experimental Crystal Structure Determination

2020

Related Article: Zijie Qiu, Sobi Asako, Yunbin Hu, Cheng-Wei Ju, Thomas Liu, Loïc Rondin, Dieter Schollmeyer, Jean-Sébastien Lauret, Klaus Müllen, Akimitsu Narita|2020|J.Am.Chem.Soc.|142|14814|doi:10.1021/jacs.0c05504

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters1823-di-t-butyl-1213-ethenocyclohepta[uvwxyz]dibenzo[45:67]cyclohepta[123-gh]phenanthro[9101-jkl]hexahelicene tetrahydrofuran solvateExperimental 3D Coordinates
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CCDC 2047540: Experimental Crystal Structure Determination

2021

Related Article: Zijie Qiu, Cheng-Wei Ju, Lucas Frédéric, Yunbin Hu, Dieter Schollmeyer, Grégory Pieters, Klaus Müllen, Akimitsu Narita|2021|J.Am.Chem.Soc.|143|4661|doi:10.1021/jacs.0c13197

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters69-di-t-butyl-114-bis(naphthalen-2-yl)tribenzo[fgijrst]pentaphene chloroform solvate hydrateExperimental 3D Coordinates
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CCDC 2004419: Experimental Crystal Structure Determination

2020

Related Article: Zijie Qiu, Sobi Asako, Yunbin Hu, Cheng-Wei Ju, Thomas Liu, Loïc Rondin, Dieter Schollmeyer, Jean-Sébastien Lauret, Klaus Müllen, Akimitsu Narita|2020|J.Am.Chem.Soc.|142|14814|doi:10.1021/jacs.0c05504

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters22'-(2'3'-bis(4-(t-butyl)phenyl)-[11':4'1''-terphenyl]-22''-diyl)-dinaphthalene chloroform solvateExperimental 3D Coordinates
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CCDC 2047541: Experimental Crystal Structure Determination

2021

Related Article: Zijie Qiu, Cheng-Wei Ju, Lucas Frédéric, Yunbin Hu, Dieter Schollmeyer, Grégory Pieters, Klaus Müllen, Akimitsu Narita|2021|J.Am.Chem.Soc.|143|4661|doi:10.1021/jacs.0c13197

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2023-di-t-butyldibenzo[56:78]pentapheno[1141312-ijklmno]heptahelicene chloroform solvateExperimental 3D Coordinates
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CCDC 2000869: Experimental Crystal Structure Determination

2020

Related Article: Marcel Dillenburger, Zijie Qiu, Cheng-Wei Ju, Beate Müller, Svenja Morsbach, Dieter Schollmeyer, Akimitsu Narita, Klaus Müllen|2020|J.Am.Chem.Soc.|142|12916|doi:10.1021/jacs.0c04956

Space GroupCrystallography123456-hexacyclohexylcyclohexaneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2004420: Experimental Crystal Structure Determination

2020

Related Article: Zijie Qiu, Sobi Asako, Yunbin Hu, Cheng-Wei Ju, Thomas Liu, Loïc Rondin, Dieter Schollmeyer, Jean-Sébastien Lauret, Klaus Müllen, Akimitsu Narita|2020|J.Am.Chem.Soc.|142|14814|doi:10.1021/jacs.0c05504

Space GroupCrystallographyCrystal SystemCrystal Structure3-t-butyl-24-(4-t-butylphenyl)-2223-(metheno)dibenzo[bgh]benzo[67]pleiadeno[321-no]pleiadene chloroform solvateCell ParametersExperimental 3D Coordinates
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CCDC 2000868: Experimental Crystal Structure Determination

2020

Related Article: Marcel Dillenburger, Zijie Qiu, Cheng-Wei Ju, Beate Müller, Svenja Morsbach, Dieter Schollmeyer, Akimitsu Narita, Klaus Müllen|2020|J.Am.Chem.Soc.|142|12916|doi:10.1021/jacs.0c04956

Hexacyclohexylbenzene chloroform solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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